ALLIUM

Manufacturer: STANDARD HOMEOPATHIC COMPANY
Effective date: 2021-10-14
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 22:32:21

Label at a glance#

ProductALLIUM

Active ingredientALLIUM CEPA WHOLE

Label structure8 sections

Dosage and administration

Adults: Dissolve 4 tablets under tongue 4 times a day. Children: Consult a healthcare professional

Contacts and useful links#

PhoneLabel contact800-624-9659

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Made according to the
Homeopathic Pharmacopoeia
of the United States since 1903.

Warnings

WARNINGS SECTION

SPL UNCLASSIFIED SECTION

Do not use if cap band is missing or broken.

SPL UNCLASSIFIED SECTION

If you are pregnant or nursing, consult a licensed health
care professional before using this product.

SPL UNCLASSIFIED SECTION

If symptoms persist for 7 days or worsen,
contact a licensed practitioner.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP THIS AND ALL MEDICINES OUT OF THE REACH OF CHILDREN.

SPL UNCLASSIFIED SECTION

To be used according to label indications and/or
standard homeopathic indications.

OTC - QUESTIONS SECTION

Standard Homeopathic Company
Los Angeles, CA 90061
Questions? 800-624-9659

Directions

DOSAGE & ADMINISTRATION SECTION

Adults: Dissolve 4 tablets under tongue 4 times a day.
Children: Consult a healthcare professional

INACTIVE INGREDIENT SECTION

In a base of Acacia Gum and Lactose N.F.

OTC - ACTIVE INGREDIENT SECTION

ALLIUM CEPA 6X

INDICATIONS & USAGE SECTION

RUNNY NOSE,COLD OR HAY FEVER

OTC - PURPOSE SECTION

RUNNY NOSE,COLD OR HAY FEVER

Principal Display Panel -- 250 Tablet Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Standard

Homeopathic

Made in the USA Since 1903

NDC # 0360-0015-01

Homeopathic Medicine

ALLIUM CEPA

RUNNY NOSE,COLD OR HAY

FEVER*

*Claims based on traditional homeopathic

practice, not accepted medical evidence.

Not FDA evaluated.

250 TABLETS

label

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

ALLIUM
ALLIUM CEPA
ACACIA
LACTOSE MONOHYDRATE
ALLIUM CEPA WHOLE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0360-0015	0360-0015-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ACACIA	5C5403N26O	IACT
LACTOSE MONOHYDRATE	EWQ57Q8I5X	IACT
ALLIUM CEPA WHOLE	8P2VLG2456	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ce512373-2e00-219d-e053-2995a90ad9d5			49db3bce-00bf-32a0-e054-00144ff8d46c	2021-10-14	Warnings	Exact identifier spl id: ce512373-2e00-219d-e053-2995a90ad9d5 spl set id: 49db3bce-00bf-32a0-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.